SI1863812T1 - Dipeptidyl peptidase-iv inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as an active agent - Google Patents
Dipeptidyl peptidase-iv inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as an active agentInfo
- Publication number
- SI1863812T1 SI1863812T1 SI200331873T SI200331873T SI1863812T1 SI 1863812 T1 SI1863812 T1 SI 1863812T1 SI 200331873 T SI200331873 T SI 200331873T SI 200331873 T SI200331873 T SI 200331873T SI 1863812 T1 SI1863812 T1 SI 1863812T1
- Authority
- SI
- Slovenia
- Prior art keywords
- same
- preparing
- methods
- pharmaceutical compositions
- active agent
- Prior art date
Links
- 102000016622 Dipeptidyl Peptidase 4 Human genes 0.000 title 1
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 title 1
- 239000013543 active substance Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4436—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Diabetes (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Child & Adolescent Psychology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20050027756 | 2005-04-01 | ||
| KR20050053761 | 2005-06-22 | ||
| KR20050085980 | 2005-09-15 | ||
| KR20050122361 | 2005-12-13 | ||
| PCT/KR2006/001169 WO2006104356A1 (en) | 2005-04-01 | 2006-03-30 | Dipeptidyl peptidase-iv inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as an active agent |
| EP06732744A EP1863812B1 (en) | 2005-04-01 | 2006-03-30 | Dipeptidyl peptidase-iv inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as an active agent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI1863812T1 true SI1863812T1 (en) | 2010-11-30 |
Family
ID=37053586
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI200331873T SI1863812T1 (en) | 2005-04-01 | 2006-03-30 | Dipeptidyl peptidase-iv inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as an active agent |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US7879848B2 (en) |
| EP (1) | EP1863812B1 (en) |
| JP (1) | JP4977685B2 (en) |
| KR (3) | KR100776623B1 (en) |
| CN (1) | CN101151265B (en) |
| AR (1) | AR053195A1 (en) |
| AT (1) | ATE473976T1 (en) |
| AU (1) | AU2006229520B2 (en) |
| BR (1) | BRPI0609424B8 (en) |
| CA (1) | CA2602248C (en) |
| DE (1) | DE602006015443D1 (en) |
| DK (1) | DK1863812T3 (en) |
| EA (1) | EA012591B1 (en) |
| ES (1) | ES2349178T3 (en) |
| IL (1) | IL185479A (en) |
| MA (1) | MA29586B1 (en) |
| MX (1) | MX2007012175A (en) |
| MY (1) | MY150102A (en) |
| NZ (1) | NZ560789A (en) |
| PE (1) | PE20061354A1 (en) |
| PL (1) | PL1863812T3 (en) |
| PT (1) | PT1863812E (en) |
| SI (1) | SI1863812T1 (en) |
| TW (1) | TWI357902B (en) |
| UA (1) | UA89396C2 (en) |
| UY (1) | UY29448A1 (en) |
| WO (1) | WO2006104356A1 (en) |
| ZA (1) | ZA200708304B (en) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007148185A2 (en) | 2006-06-21 | 2007-12-27 | Pfizer Products Inc. | Substituted 3 -amino- pyrrolidino-4 -lactams as dpp inhibitors |
| AU2007283113A1 (en) | 2006-08-08 | 2008-02-14 | Sanofi-Aventis | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use |
| KR20120030570A (en) | 2007-04-03 | 2012-03-28 | 미쓰비시 타나베 파마 코퍼레이션 | Combined use of dipeptidyl peptidase iv inhibitor compound and sweetener |
| CN101357922B (en) * | 2007-08-02 | 2011-05-18 | 山东轩竹医药科技有限公司 | New DPP-IV Inhibitors |
| EP2025674A1 (en) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituted tetra hydro naphthalines, method for their manufacture and their use as drugs |
| AU2008333110A1 (en) * | 2007-12-05 | 2009-06-11 | Astrazeneca Ab (Publ) | New compounds III |
| AU2008341352B2 (en) * | 2007-12-21 | 2013-08-01 | Lg Chem, Ltd. | Dipeptidyl peptidase-IV inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as active agent |
| CL2008003653A1 (en) | 2008-01-17 | 2010-03-05 | Mitsubishi Tanabe Pharma Corp | Use of a glucopyranosyl-derived sglt inhibitor and a selected dppiv inhibitor to treat diabetes; and pharmaceutical composition. |
| CN101486689B (en) * | 2008-01-18 | 2011-08-10 | 山东轩竹医药科技有限公司 | DPP-IV inhibitor with sulfonamide formamide piperazine structure |
| UY31968A (en) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | NEW HETEROCYCLIC DERIVATIVES, THEIR PROCESSES FOR THEIR PREPARATION, AND THEIR THERAPEUTIC USES |
| JO2870B1 (en) * | 2008-11-13 | 2015-03-15 | ميرك شارب اند دوهم كورب | Aminotetrahydropyrans as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| CA2754712A1 (en) * | 2009-03-13 | 2010-09-16 | Sun Chemical B.V. | Cyclic carbamate compounds useful in energy-curable compositions |
| BR112012003973A2 (en) | 2009-08-26 | 2015-09-08 | Sanofi Sa | crystalline heteroaromatic fluoroglycoside hydrates, pharmaceuticals comprising these compounds and their use |
| US8871760B2 (en) * | 2009-09-21 | 2014-10-28 | Roche Palo Alto Llc | [1,2,4]triazolo[3,4-C][1,4]oxazines as P2X7 modulators |
| WO2011107494A1 (en) | 2010-03-03 | 2011-09-09 | Sanofi | Novel aromatic glycoside derivatives, medicaments containing said compounds, and the use thereof |
| CN102260265B (en) * | 2010-05-24 | 2015-09-02 | 上海阳帆医药科技有限公司 | Hexahydropyrrolo [3,4-b] pyrrole derivative, Its Preparation Method And Use |
| US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| EA022500B1 (en) | 2010-09-03 | 2016-01-29 | Эл Джи Лайф Сайенсиз Лтд. | Production method of intermediate compound for synthesizing medicament |
| TWI519533B (en) * | 2010-11-01 | 2016-02-01 | Ｌｇ生命科學有限公司 | Hydrate of 1-{(2s)-2-amino-4-(2,4-bis(trifluoromethyl)-5,8-dihydropyrido(3,4-d)pyrimidin-7(6h)-yl)-4-oxobutyl}-5,5-difluoro-piperidin-2-one tartrate |
| WO2012120052A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
| WO2012120056A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
| US8710050B2 (en) | 2011-03-08 | 2014-04-29 | Sanofi | Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120053A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683705B1 (en) | 2011-03-08 | 2015-04-22 | Sanofi | Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012170702A1 (en) | 2011-06-08 | 2012-12-13 | Arena Pharmaceuticals, Inc. | Modulators of the gpr119 receptor and the treatment of disorders related thereto |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2014064215A1 (en) | 2012-10-24 | 2014-05-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | TPL2 KINASE INHIBITORS FOR PREVENTING OR TREATING DIABETES AND FOR PROMOTING β-CELL SURVIVAL |
| CN105085528A (en) * | 2014-05-15 | 2015-11-25 | 成都贝斯凯瑞生物科技有限公司 | Aminotetrahydropyran derivative as dipeptidyl peptidase-IV inhibitor |
| EP3273981B1 (en) | 2015-03-24 | 2020-04-29 | INSERM - Institut National de la Santé et de la Recherche Médicale | Method and pharmaceutical composition for use in the treatment of diabetes |
| WO2017147312A1 (en) | 2016-02-23 | 2017-08-31 | Indiana University Research & Technology Corporation | Combination therapies for treatment of spinal muscular atrophy |
| KR102068754B1 (en) * | 2017-04-20 | 2020-01-21 | 주식회사 엘지화학 | Production Method of Intermediate Compound for Synthesizing Medicament |
| KR102184129B1 (en) * | 2017-11-16 | 2020-11-27 | 주식회사 엘지화학 | Production method of intermediate compound for synthesizing medicament |
| CN108191647B (en) * | 2018-02-22 | 2020-09-29 | 江苏尚莱特医药化工材料有限公司 | Synthesis method of 2, 2-difluoro dicarboxylic acid dialkyl ester |
| CN111537622B (en) * | 2019-11-29 | 2021-11-26 | 杭州华东医药集团新药研究院有限公司 | Method for detecting impurities of duloxetine and salts thereof |
| KR20250097733A (en) | 2023-12-21 | 2025-06-30 | 이니스트에스티 주식회사 | Novel Salt Of Dipeptidyl Peptidase-IV (DPP-IV) Inhibitor, Method For Preparing Thereof, and Pharmaceutical Composition Comprising Thereof |
| KR20250137744A (en) | 2024-03-11 | 2025-09-19 | 엠에프씨 주식회사 | Novel crystalline form and its preparation method thereof |
| KR20250147756A (en) | 2024-03-27 | 2025-10-14 | 엠에프씨 주식회사 | A novel form of gemigliptin malate crystalline form and its preparation method |
| KR20250155700A (en) | 2024-04-24 | 2025-10-31 | 주식회사 다산제약 | Prepartion method of Gemigliptin and composition for inhibiting DPP-4 comprising the same |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CO5150173A1 (en) | 1998-12-10 | 2002-04-29 | Novartis Ag | COMPOUNDS N- (REPLACED GLYCLE) -2-DIPEPTIDYL-IV PEPTIDASE INHIBITING CYANOPIRROLIDINS (DPP-IV) WHICH ARE EFFECTIVE IN THE TREATMENT OF CONDITIONS MEDIATED BY DPP-IV INHIBITION |
| UA74912C2 (en) | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
| US6861440B2 (en) * | 2001-10-26 | 2005-03-01 | Hoffmann-La Roche Inc. | DPP IV inhibitors |
| WO2003057144A2 (en) * | 2001-12-26 | 2003-07-17 | Guilford Pharmaceuticals | Change inhibitors of dipeptidyl peptidase iv |
| US7307164B2 (en) * | 2002-03-25 | 2007-12-11 | Merck & Co., Inc. | β-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CA2483843A1 (en) * | 2002-04-29 | 2003-11-13 | Merck & Co. Inc. | Tetrahydropyranyl cyclopentyl tetrahydroisoquinoline modulators of chemokine receptor activity |
| JP4530852B2 (en) * | 2002-07-15 | 2010-08-25 | メルク・シャープ・エンド・ドーム・コーポレイション | Piperidinopyrimidine dipeptidyl peptidase inhibitors for the treatment of diabetes |
| JP2004285325A (en) * | 2002-12-17 | 2004-10-14 | Fuji Photo Film Co Ltd | Method for forming pattern and material for material adhesion pattern |
| CA2508947A1 (en) * | 2002-12-20 | 2004-07-15 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| US7265128B2 (en) * | 2003-01-17 | 2007-09-04 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CA2513684A1 (en) | 2003-01-31 | 2004-08-19 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| EP1732885A1 (en) * | 2004-02-23 | 2006-12-20 | Trustees Of Tufts College | Lactams as conformationally constrained peptidomimetic inhibitors |
| US7291427B2 (en) * | 2004-03-19 | 2007-11-06 | Fujifilm Corporation | Surface graft material, conductive pattern material, and production method thereof |
| DE102004020908A1 (en) * | 2004-04-28 | 2005-11-17 | Grünenthal GmbH | Substituted 5,6,7,8-tetrahydropyrido [4,3-d] pyrimidin-2-yl and 5,6,7,8-tetrahydroquinazolin-2-yl compounds |
| DE102005016170A1 (en) * | 2005-04-07 | 2006-10-12 | Grünenthal GmbH | 4,5,6,7-tetrahydro-isoxazolo (4,5c) pyridine compounds and their use for the preparation of medicaments |
| ZA200709961B (en) * | 2005-05-10 | 2009-07-29 | Vertex Pharma | Bicyclic derivatives as modulators of ion channels |
| JP2009537558A (en) * | 2006-05-16 | 2009-10-29 | スミスクライン・ビーチャム・コーポレイション | Prolyl hydroxylase inhibitor |
| EP2229395A1 (en) * | 2008-01-17 | 2010-09-22 | Grünenthal GmbH | Substituted sulfonamide derivatives |
-
2006
- 2006-03-21 TW TW095109718A patent/TWI357902B/en active
- 2006-03-29 AR ARP060101214A patent/AR053195A1/en active IP Right Grant
- 2006-03-30 PL PL06732744T patent/PL1863812T3/en unknown
- 2006-03-30 AU AU2006229520A patent/AU2006229520B2/en active Active
- 2006-03-30 UA UAA200710765A patent/UA89396C2/en unknown
- 2006-03-30 MY MYPI20061446A patent/MY150102A/en unknown
- 2006-03-30 KR KR1020060029138A patent/KR100776623B1/en active Active
- 2006-03-30 DE DE602006015443T patent/DE602006015443D1/en active Active
- 2006-03-30 DK DK06732744.5T patent/DK1863812T3/en active
- 2006-03-30 PE PE2006000351A patent/PE20061354A1/en active IP Right Grant
- 2006-03-30 ES ES06732744T patent/ES2349178T3/en active Active
- 2006-03-30 CA CA2602248A patent/CA2602248C/en active Active
- 2006-03-30 WO PCT/KR2006/001169 patent/WO2006104356A1/en not_active Ceased
- 2006-03-30 UY UY29448A patent/UY29448A1/en not_active Application Discontinuation
- 2006-03-30 EA EA200701854A patent/EA012591B1/en unknown
- 2006-03-30 NZ NZ560789A patent/NZ560789A/en unknown
- 2006-03-30 EP EP06732744A patent/EP1863812B1/en active Active
- 2006-03-30 US US11/910,370 patent/US7879848B2/en active Active
- 2006-03-30 PT PT06732744T patent/PT1863812E/en unknown
- 2006-03-30 CN CN200680009935XA patent/CN101151265B/en active Active
- 2006-03-30 BR BRPI0609424A patent/BRPI0609424B8/en active IP Right Grant
- 2006-03-30 MX MX2007012175A patent/MX2007012175A/en active IP Right Grant
- 2006-03-30 JP JP2008503954A patent/JP4977685B2/en active Active
- 2006-03-30 AT AT06732744T patent/ATE473976T1/en active
- 2006-03-30 SI SI200331873T patent/SI1863812T1/en unknown
-
2007
- 2007-08-23 IL IL185479A patent/IL185479A/en active IP Right Grant
- 2007-08-28 KR KR1020070086486A patent/KR100794184B1/en active Active
- 2007-08-28 KR KR1020070086444A patent/KR100830902B1/en active Active
- 2007-09-28 ZA ZA200708304A patent/ZA200708304B/en unknown
- 2007-10-30 MA MA30343A patent/MA29586B1/en unknown
Also Published As
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